Hsu Ping-Ching, Lan Renny S, Brasky Theodore M, Marian Catalin, Cheema Amrita K, Ressom Habtom W, Loffredo Christopher A, Pickworth Wallace B, Shields Peter G
Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio.
Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Cancer Epidemiol Biomarkers Prev. 2017 Jan;26(1):51-60. doi: 10.1158/1055-9965.EPI-16-0124. Epub 2016 Sep 14.
The use of menthol in cigarettes and marketing is under consideration for regulation by the FDA. However, the effects of menthol on smoking behavior and carcinogen exposure have been inconclusive. We previously reported metabolomic profiling for cigarette smokers, and novelly identified a menthol-glucuronide (MG) as the most significant metabolite directly related to smoking. Here, MG is studied in relation to smoking behavior and metabolomic profiles.
This is a cross-sectional study of 105 smokers who smoked two cigarettes in the laboratory one hour apart. Blood nicotine, MG, and exhaled carbon monoxide (CO) boosts were determined (the difference before and after smoking). Spearman correlation, χ, and ANCOVA adjusted for gender, race, and cotinine levels for menthol smokers assessed the relationship of MG boost, smoking behavior, and metabolic profiles. Multivariate metabolite characterization using supervised partial least squares-discriminant analysis (PLS-DA) was carried out for the classification of metabolomics profiles.
MG boost was positively correlated with CO boost, nicotine boost, average puff volume, puff duration, and total smoke exposure. Classification using PLS-DA, MG was the top metabolite discriminating metabolome of menthol versus nonmenthol smokers. Among menthol smokers, 42 metabolites were significantly correlated with MG boost, which linked to cellular functions, such as of cell death, survival, and movement.
Plasma MG boost is a new smoking behavior biomarker that may provide novel information over self-reported use of menthol cigarettes by integrating different smoking measures for understanding smoking behavior and harm of menthol cigarettes.
These results provide insight into the biological effect of menthol smoking. Cancer Epidemiol Biomarkers Prev; 26(1); 51-60. ©2016 AACR.
美国食品药品监督管理局(FDA)正在考虑对香烟中薄荷醇的使用及其营销进行监管。然而,薄荷醇对吸烟行为和致癌物暴露的影响尚无定论。我们之前报道了吸烟者的代谢组学分析,并首次鉴定出薄荷醇葡糖苷酸(MG)是与吸烟直接相关的最重要代谢物。在此,我们对MG与吸烟行为和代谢组学特征的关系进行了研究。
这是一项横断面研究,105名吸烟者在实验室中每隔一小时吸两支香烟。测定血液中的尼古丁、MG以及呼出一氧化碳(CO)的增加值(吸烟前后的差值)。对于薄荷醇吸烟者,采用Spearman相关性分析、χ检验以及调整了性别、种族和可替宁水平的协方差分析来评估MG增加值、吸烟行为和代谢特征之间的关系。使用有监督的偏最小二乘判别分析(PLS-DA)进行多变量代谢物表征,以对代谢组学特征进行分类。
MG增加值与CO增加值、尼古丁增加值、平均吸量、吸程和总烟雾暴露呈正相关。使用PLS-DA进行分类时,MG是区分薄荷醇吸烟者与非薄荷醇吸烟者代谢组的首要代谢物。在薄荷醇吸烟者中,42种代谢物与MG增加值显著相关,这些代谢物与细胞死亡、存活和运动等细胞功能相关。
血浆MG增加值是一种新的吸烟行为生物标志物,通过整合不同的吸烟测量指标来理解薄荷醇香烟的吸烟行为和危害,可能比自我报告的薄荷醇香烟使用情况提供更多新信息。
这些结果为薄荷醇吸烟的生物学效应提供了见解。《癌症流行病学、生物标志物与预防》;26(1);51 - 60。©2016美国癌症研究协会。